메뉴 건너뛰기




Volumn 74, Issue 24, 2014, Pages 7475-7486

Syntheses and discovery of a novel class of cinnamic hydroxamates as histone deacetylase inhibitors by multimodality molecular imaging in living subjects

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; CYCLIN DEPENDENT KINASE INHIBITOR 1; FLUORODEOXYGLUCOSE F 18; HEAT SHOCK PROTEIN 90; HEAT SHOCK PROTEIN 90 INHIBITOR; HISTONE DEACETYLASE 6; HISTONE DEACETYLASE INHIBITOR; HISTONE H3; HYDRAZONE DERIVATIVE; HYDROXAMIC ACID DERIVATIVE; KETONE; METHYL 3 [4 [2 (2 BROMO 3 PHENYLALLYLIDENE)HYDRAZINECARBONYL]PHENYL]PROPANOATE; PROTEIN P23; UNCLASSIFIED DRUG; CINNAMIC ACID; CINNAMIC ACID DERIVATIVE; HDAC6 PROTEIN, HUMAN; HISTONE DEACETYLASE; HYDROXAMIC ACID;

EID: 84918530742     PISSN: 00085472     EISSN: 15387445     Source Type: Journal    
DOI: 10.1158/0008-5472.CAN-14-0197     Document Type: Article
Times cited : (10)

References (49)
  • 1
    • 67650090545 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: Potential in cancer therapy
    • Marks PA, Xu WS. Histone deacetylase inhibitors: potential in cancer therapy. J Cell Biochem 2009;107:600-8.
    • (2009) J Cell Biochem , vol.107 , pp. 600-608
    • Marks, P.A.1    Xu, W.S.2
  • 4
    • 73949128107 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors in cancer therapy
    • Lane AA, Chabner BA. Histone deacetylase inhibitors in cancer therapy. J Clin Oncol 2009;27:5459-68.
    • (2009) J Clin Oncol , vol.27 , pp. 5459-5468
    • Lane, A.A.1    Chabner, B.A.2
  • 5
    • 77649171884 scopus 로고    scopus 로고
    • Novel histone deacetylase inhibitors in clinical trials as anti-cancer agents
    • Tan J, Cang S, Ma Y, Petrillo RL, Liu D. Novel histone deacetylase inhibitors in clinical trials as anti-cancer agents. J Hematol Oncol 2010;3:5.
    • (2010) J Hematol Oncol , vol.3 , pp. 5
    • Tan, J.1    Cang, S.2    Ma, Y.3    Petrillo, R.L.4    Liu, D.5
  • 6
    • 79958719758 scopus 로고    scopus 로고
    • HDAC inhibitor vorinostat enhances the antitumor effect of gefitinib in squamous cell carcinoma of head and neck by modulating ErbB receptor expression and reverting EMT
    • Bruzzese F, Leone A, Rocco M, Carbone C, Piro G, Caraglia M, et al. HDAC inhibitor vorinostat enhances the antitumor effect of gefitinib in squamous cell carcinoma of head and neck by modulating ErbB receptor expression and reverting EMT. J Cell Physiol 2011;226:2378-90.
    • (2011) J Cell Physiol , vol.226 , pp. 2378-2390
    • Bruzzese, F.1    Leone, A.2    Rocco, M.3    Carbone, C.4    Piro, G.5    Caraglia, M.6
  • 7
    • 84859538161 scopus 로고    scopus 로고
    • Phase II trial of vorinostat in combination with bortezomib in recurrent glioblastoma: A north central cancer treatment group study
    • Friday BB, Anderson SK, Buckner J, Yu C, Giannini C, Geoffroy F, et al. Phase II trial of vorinostat in combination with bortezomib in recurrent glioblastoma: a north central cancer treatment group study. Neuro Oncol 2012;14:215-21.
    • (2012) Neuro Oncol , vol.14 , pp. 215-221
    • Friday, B.B.1    Anderson, S.K.2    Buckner, J.3    Yu, C.4    Giannini, C.5    Geoffroy, F.6
  • 8
    • 79551490303 scopus 로고    scopus 로고
    • The emerging role of histone deacetylase inhibitors in treating T-cell lymphomas
    • Horwitz SM. The emerging role of histone deacetylase inhibitors in treating T-cell lymphomas. Curr Hematol Malig Rep 2011;6:67-72.
    • (2011) Curr Hematol Malig Rep , vol.6 , pp. 67-72
    • Horwitz, S.M.1
  • 9
    • 79956125729 scopus 로고    scopus 로고
    • Deciphering the molecular events necessary for synergistic tumor cell apoptosis mediated by the histone deacetylase inhibitor vorinostat and the BH3 mimetic ABT-737
    • Wiegmans AP, Alsop AE, Bots M, Cluse LA, Williams SP, Banks K-M, et al. Deciphering the molecular events necessary for synergistic tumor cell apoptosis mediated by the histone deacetylase inhibitor vorinostat and the BH3 mimetic ABT-737. Cancer Res 2011;71:3603-15.
    • (2011) Cancer Res , vol.71 , pp. 3603-3615
    • Wiegmans, A.P.1    Alsop, A.E.2    Bots, M.3    Cluse, L.A.4    Williams, S.P.5    Banks, K.-M.6
  • 10
    • 84871407100 scopus 로고    scopus 로고
    • Phase 1 clinical trial of the novel proteasome inhibitor marizomib with the histone deacetylase inhibitor vorinostat in patients with melanoma, pancreatic and lung cancer based on in vitro assessments of the combination
    • Millward M, Price T, Townsend A, Sweeney C, Spencer A, Sukumaran S, et al. Phase 1 clinical trial of the novel proteasome inhibitor marizomib with the histone deacetylase inhibitor vorinostat in patients with melanoma, pancreatic and lung cancer based on in vitro assessments of the combination. Invest New Drugs 2012; 30:2303-17.
    • (2012) Invest New Drugs , vol.30 , pp. 2303-2317
    • Millward, M.1    Price, T.2    Townsend, A.3    Sweeney, C.4    Spencer, A.5    Sukumaran, S.6
  • 11
    • 79952158522 scopus 로고    scopus 로고
    • Rational therapeutic combinations with histone deacetylase inhibitors for the treatment of cancer
    • Thurn KT, Thomas S, Moore A, Munster PN. Rational therapeutic combinations with histone deacetylase inhibitors for the treatment of cancer. Future Oncol 2011;7:263-83.
    • (2011) Future Oncol , vol.7 , pp. 263-283
    • Thurn, K.T.1    Thomas, S.2    Moore, A.3    Munster, P.N.4
  • 12
    • 78650321835 scopus 로고    scopus 로고
    • Novel chimeric histone deacetylase inhibitors: A series of lapatinib hybrides as potent inhibitors of epidermal growth factor receptor (EGFR),human epidermal growth factor receptor 2 (HER2), and histone deacetylase activity
    • Mahboobi S, Sellmer A, Winkler M, Eichhorn E, Pongratz H, Ciossek T, et al. Novel chimeric histone deacetylase inhibitors: a series of lapatinib hybrides as potent inhibitors of epidermal growth factor receptor (EGFR),human epidermal growth factor receptor 2 (HER2), and histone deacetylase activity. J Med Chem 2010;53:8546-55.
    • (2010) J Med Chem , vol.53 , pp. 8546-8555
    • Mahboobi, S.1    Sellmer, A.2    Winkler, M.3    Eichhorn, E.4    Pongratz, H.5    Ciossek, T.6
  • 13
    • 78649527328 scopus 로고    scopus 로고
    • An aldol-based build/couple/pair strategy for the synthesis of medium- and large-sized rings: Discovery of macrocyclic histone deacetylase inhibitors
    • Marcaurelle LA, Comer E, Dandapani S, Duvall JR, Gerard B, Kesavan S, et al. An aldol-based build/couple/pair strategy for the synthesis of medium- and large-sized rings: discovery of macrocyclic histone deacetylase inhibitors. J Am Chem Soc 2010;132:16962-76.
    • (2010) J Am Chem Soc , vol.132 , pp. 16962-16976
    • Marcaurelle, L.A.1    Comer, E.2    Dandapani, S.3    Duvall, J.R.4    Gerard, B.5    Kesavan, S.6
  • 14
    • 77955866855 scopus 로고    scopus 로고
    • Non-peptide macrocyclic histone deacetylase inhibitors derived from tricyclic ketolide skeleton
    • Mwakwari SC, Guerrant W, Patil V, Khan SI, Tekwani BL, Gurard-Levin ZA, et al. Non-peptide macrocyclic histone deacetylase inhibitors derived from tricyclic ketolide skeleton. J Med Chem 2010;53:6100-11.
    • (2010) J Med Chem , vol.53 , pp. 6100-6111
    • Mwakwari, S.C.1    Guerrant, W.2    Patil, V.3    Khan, S.I.4    Tekwani, B.L.5    Gurard-Levin, Z.A.6
  • 15
    • 77950679234 scopus 로고    scopus 로고
    • A structure-based virtual screening approach toward the discovery of histone deacetylase inhibitors: Identification of promising zinc-chelating groups
    • Park H, Kim S, Kim YE, Lim SJ. A structure-based virtual screening approach toward the discovery of histone deacetylase inhibitors: identification of promising zinc-chelating groups. ChemMedChem 2010;5:591-7.
    • (2010) ChemMedChem , vol.5 , pp. 591-597
    • Park, H.1    Kim, S.2    Kim, Y.E.3    Lim, S.J.4
  • 17
    • 79955455755 scopus 로고    scopus 로고
    • Development of tetrahydroisoquinoline-based hydroxamic acid derivatives: Potent histone deacetylase inhibitors with marked in vitro and in vivo antitumor activities
    • Zhang Y, Feng J, Jia Y, Wang X, Zhang L, Liu C, et al. Development of tetrahydroisoquinoline-based hydroxamic acid derivatives: potent histone deacetylase inhibitors with marked in vitro and in vivo antitumor activities. J Med Chem 2011;54:2823-38.
    • (2011) J Med Chem , vol.54 , pp. 2823-2838
    • Zhang, Y.1    Feng, J.2    Jia, Y.3    Wang, X.4    Zhang, L.5    Liu, C.6
  • 18
    • 73249149751 scopus 로고    scopus 로고
    • HDAC6 regulates androgen receptor hypersensitivity and nuclear localization via modulating Hsp90 acetylation in castration-resistant prostate cancer
    • Ai J, Wang Y, Dar JA, Liu J, Liu L, Nelson JB, et al. HDAC6 regulates androgen receptor hypersensitivity and nuclear localization via modulating Hsp90 acetylation in castration-resistant prostate cancer. Mol Endocrinol 2009;23:1963-72.
    • (2009) Mol Endocrinol , vol.23 , pp. 1963-1972
    • Ai, J.1    Wang, Y.2    Dar, J.A.3    Liu, J.4    Liu, L.5    Nelson, J.B.6
  • 19
    • 78651304171 scopus 로고    scopus 로고
    • Carbamazepine promotes Her-2 protein degradation in breast cancer cells by modulating HDAC6 activity and acetylation of Hsp90
    • Meng Q, Chen X, Sun L, Zhao C, Sui G, Cai L. Carbamazepine promotes Her-2 protein degradation in breast cancer cells by modulating HDAC6 activity and acetylation of Hsp90. Mol Cell Biochem 2011;348:165-71.
    • (2011) Mol Cell Biochem , vol.348 , pp. 165-171
    • Meng, Q.1    Chen, X.2    Sun, L.3    Zhao, C.4    Sui, G.5    Cai, L.6
  • 20
    • 52649133274 scopus 로고    scopus 로고
    • HDAC6 inhibition enhances 17-AAG - mediated abrogation of hsp90 chaperone function in human leukemia cells
    • Rao R, Fiskus W, Yang Y, Lee P, Joshi R, Fernandez P, et al. HDAC6 inhibition enhances 17-AAG - mediated abrogation of hsp90 chaperone function in human leukemia cells. Blood 2008; 112:1886-93.
    • (2008) Blood , vol.112 , pp. 1886-1893
    • Rao, R.1    Fiskus, W.2    Yang, Y.3    Lee, P.4    Joshi, R.5    Fernandez, P.6
  • 22
    • 55749097776 scopus 로고    scopus 로고
    • Genistein down-regulates androgen receptor by modulating HDAC6-Hsp90 chaperone function
    • Basak S, Pookot D, Noonan EJ, Dahiya R. Genistein down-regulates androgen receptor by modulating HDAC6-Hsp90 chaperone function. Mol Cancer Ther 2008;7:3195-202.
    • (2008) Mol Cancer Ther , vol.7 , pp. 3195-3202
    • Basak, S.1    Pookot, D.2    Noonan, E.J.3    Dahiya, R.4
  • 23
    • 21144444486 scopus 로고    scopus 로고
    • HDAC6 regulates Hsp90 acetylation and chaperone-dependent activation of glucocorticoid receptor
    • Kovacs JJ, Murphy PJ, Gaillard S, Zhao X, Wu JT, Nicchitta CV, et al. HDAC6 regulates Hsp90 acetylation and chaperone-dependent activation of glucocorticoid receptor. Mol Cell 2005;18:601-7.
    • (2005) Mol Cell , vol.18 , pp. 601-607
    • Kovacs, J.J.1    Murphy, P.J.2    Gaillard, S.3    Zhao, X.4    Wu, J.T.5    Nicchitta, C.V.6
  • 24
    • 39149109163 scopus 로고    scopus 로고
    • Molecular imaging of the efficacy of heat shock protein 90 inhibitors in living subjects
    • Chan CT, Paulmurugan R, Gheysens OS, Kim J, Chiosis G, Gambhir SS. Molecular imaging of the efficacy of heat shock protein 90 inhibitors in living subjects. Cancer Res 2008;68:216-26.
    • (2008) Cancer Res , vol.68 , pp. 216-226
    • Chan, C.T.1    Paulmurugan, R.2    Gheysens, O.S.3    Kim, J.4    Chiosis, G.5    Gambhir, S.S.6
  • 25
    • 84866272310 scopus 로고    scopus 로고
    • Discovery and validation of small-molecule heat-shock protein 90 inhibitors through multimodality molecular imaging in living subjects
    • Chan CT, Reeves RE, Geller R, Yaghoubi SS, Hoehne A, Solow-Cordero DE, et al. Discovery and validation of small-molecule heat-shock protein 90 inhibitors through multimodality molecular imaging in living subjects. Proc Natl Acad Sci 2012;109:E2476-E85.
    • (2012) Proc Natl Acad Sci , vol.109 , pp. E2476-E2485
    • Chan, C.T.1    Reeves, R.E.2    Geller, R.3    Yaghoubi, S.S.4    Hoehne, A.5    Solow-Cordero, D.E.6
  • 26
    • 33745174538 scopus 로고    scopus 로고
    • Heat shock protein-90 inhibitors: A chronicle from geldanamycin to today's agents
    • Chiosis G, Caldas Lopes E, Solit D. Heat shock protein-90 inhibitors: a chronicle from geldanamycin to today's agents. Curr Opin Investig Drugs 2006;7:534-41.
    • (2006) Curr Opin Investig Drugs , vol.7 , pp. 534-541
    • Chiosis, G.1    Caldas Lopes, E.2    Solit, D.3
  • 28
    • 3242722132 scopus 로고    scopus 로고
    • A time-resolved fluorescence resonance energy transfer-based HTS assay and a surface plasmon resonance-based binding assay for heat shock protein 90 inhibitors
    • Zhou V, Han S, Brinker A, Klock H, Caldwell J, Gu X-j. A time-resolved fluorescence resonance energy transfer-based HTS assay and a surface plasmon resonance-based binding assay for heat shock protein 90 inhibitors. Anal Biochem 2004;331:349-57.
    • (2004) Anal Biochem , vol.331 , pp. 349-357
    • Zhou, V.1    Han, S.2    Brinker, A.3    Klock, H.4    Caldwell, J.5    Gu, X.-J.6
  • 29
    • 33748101201 scopus 로고    scopus 로고
    • Consensus guided mutagenesis of Renilla luciferase yields enhanced stability and light output
    • Loening AM, Fenn TD, Wu AM, Gambhir SS. Consensus guided mutagenesis of Renilla luciferase yields enhanced stability and light output. Protein Eng Des Sel 2006;19:391-400.
    • (2006) Protein Eng des Sel , vol.19 , pp. 391-400
    • Loening, A.M.1    Fenn, T.D.2    Wu, A.M.3    Gambhir, S.S.4
  • 30
    • 80053357507 scopus 로고    scopus 로고
    • Molecular basis for the actions of Hsp90 inhibitors and cancer therapy
    • Yamaki H, Nakajima M, Shimotohno KW, Tanaka N. Molecular basis for the actions of Hsp90 inhibitors and cancer therapy. J Antibiot 2011;64:635-44.
    • (2011) J Antibiot , vol.64 , pp. 635-644
    • Yamaki, H.1    Nakajima, M.2    Shimotohno, K.W.3    Tanaka, N.4
  • 31
    • 65549166880 scopus 로고    scopus 로고
    • HDAC6 modulates Hsp90 chaperone activity and regulates activation of aryl hydrocarbon receptor signaling
    • Kekatpure VD, Dannenberg AJ, Subbaramaiah K. HDAC6 modulates Hsp90 chaperone activity and regulates activation of aryl hydrocarbon receptor signaling. J Biol Chem 2009;284:7436-45.
    • (2009) J Biol Chem , vol.284 , pp. 7436-7445
    • Kekatpure, V.D.1    Dannenberg, A.J.2    Subbaramaiah, K.3
  • 32
    • 0344640906 scopus 로고    scopus 로고
    • Domain-selective small-molecule inhibitor of histone deacetylase 6 (HDAC6)-mediated tubulin deacetylation
    • Haggarty SJ, Koeller KM, Wong JC, Grozinger CM, Schreiber SL. Domain-selective small-molecule inhibitor of histone deacetylase 6 (HDAC6)-mediated tubulin deacetylation. Proc Natl Acad Sci 2003; 100:4389-94.
    • (2003) Proc Natl Acad Sci , vol.100 , pp. 4389-4394
    • Haggarty, S.J.1    Koeller, K.M.2    Wong, J.C.3    Grozinger, C.M.4    Schreiber, S.L.5
  • 33
    • 0038274087 scopus 로고    scopus 로고
    • Structural biasing elements for in-cell histone deacetylase paralog selectivity
    • Wong JC, Hong R, Schreiber SL. Structural biasing elements for in-cell histone deacetylase paralog selectivity. J Am Chem Soc 2003;125:5586-7.
    • (2003) J Am Chem Soc , vol.125 , pp. 5586-5587
    • Wong, J.C.1    Hong, R.2    Schreiber, S.L.3
  • 34
    • 77953081930 scopus 로고    scopus 로고
    • The influence of mediators of intracellular trafficking on transgene expression efficacy of polymer-plasmidDNAcomplexes
    • Barua S, Rege K. The influence of mediators of intracellular trafficking on transgene expression efficacy of polymer-plasmidDNAcomplexes. Biomaterials 2010;31:5894-902.
    • (2010) Biomaterials , vol.31 , pp. 5894-5902
    • Barua, S.1    Rege, K.2
  • 36
    • 67650541859 scopus 로고    scopus 로고
    • Tubacin kills Epstein-Barr virus (EBV)-Burkitt lymphoma cells by inducing reactive oxygen species and EBV lymphoblastoid cells by inducing apoptosis
    • Kawada J, Zou P, Mazitschek R, Bradner JE, Cohen JI. Tubacin kills Epstein-Barr virus (EBV)-Burkitt lymphoma cells by inducing reactive oxygen species and EBV lymphoblastoid cells by inducing apoptosis. J Biol Chem 2009;284:17102-9.
    • (2009) J Biol Chem , vol.284 , pp. 17102-17109
    • Kawada, J.1    Zou, P.2    Mazitschek, R.3    Bradner, J.E.4    Cohen, J.I.5
  • 37
    • 78650575875 scopus 로고    scopus 로고
    • Selective inhibition of histone deacetylase 6 (HDAC6) induces DNA damage and sensitizes transformed cells to anticancer agents
    • Namdar M, Perez G, Ngo L, Marks PA. Selective inhibition of histone deacetylase 6 (HDAC6) induces DNA damage and sensitizes transformed cells to anticancer agents. Proc Natl Acad Sci U S A 2010;107:20003-8.
    • (2010) Proc Natl Acad Sci U S A , vol.107 , pp. 20003-20008
    • Namdar, M.1    Perez, G.2    Ngo, L.3    Marks, P.A.4
  • 39
    • 33947594149 scopus 로고    scopus 로고
    • Structural requirements of HDAC inhibitors: SAHA analogs functionalized adjacent to the hydroxamic acid
    • Bieliauskas AV, Weerasinghe SVW, Pflum MKH. Structural requirements of HDAC inhibitors: SAHA analogs functionalized adjacent to the hydroxamic acid. Bioorg Med Chem Lett 2007;17:2216-9.
    • (2007) Bioorg Med Chem Lett , vol.17 , pp. 2216-2219
    • Bieliauskas, A.V.1    Weerasinghe, S.V.W.2    Pflum, M.K.H.3
  • 40
    • 27744496468 scopus 로고    scopus 로고
    • Non-hydroxamate histone deacetylase inhibitors
    • Suzuki T, Miyata N. Non-hydroxamate histone deacetylase inhibitors. Curr Med Chem 2005;12:2867-80.
    • (2005) Curr Med Chem , vol.12 , pp. 2867-2880
    • Suzuki, T.1    Miyata, N.2
  • 41
    • 0037039437 scopus 로고    scopus 로고
    • Optical imaging of Renilla luciferase reporter gene expression in living mice
    • Bhaumik S, Gambhir SS. Optical imaging of Renilla luciferase reporter gene expression in living mice. Proc Natl Acad Sci U S A 2002; 99:377-82.
    • (2002) Proc Natl Acad Sci U S A , vol.99 , pp. 377-382
    • Bhaumik, S.1    Gambhir, S.S.2
  • 42
    • 82855171532 scopus 로고    scopus 로고
    • Radiopharmaceutical research and production in Brazil: A 30-year history of participation in the nuclear medicine scenario
    • Santos-Oliveira R, Antunes LJ. Radiopharmaceutical research and production in Brazil: A 30-year history of participation in the nuclear medicine scenario. J Nucl Med Technol 2011;39:237-9.
    • (2011) J Nucl Med Technol , vol.39 , pp. 237-239
    • Santos-Oliveira, R.1    Antunes, L.J.2
  • 43
    • 77749246666 scopus 로고    scopus 로고
    • Evaluation of the spatial dependence of the point spread function in 2D PET image reconstruction using LOR-OSEM
    • Wiant D, Gersh JA, Bennett M, Bourland JD. Evaluation of the spatial dependence of the point spread function in 2D PET image reconstruction using LOR-OSEM. Med Phys 2010;37:1169-82.
    • (2010) Med Phys , vol.37 , pp. 1169-1182
    • Wiant, D.1    Gersh, J.A.2    Bennett, M.3    Bourland, J.D.4
  • 45
    • 66149154689 scopus 로고    scopus 로고
    • PET/CT for therapy response assessment in lymphoma
    • Hutchings M, Barrington SF. PET/CT for therapy response assessment in lymphoma. J Nucl Med 2009;50:21S-30S.
    • (2009) J Nucl Med , vol.50 , pp. 21S-30S
    • Hutchings, M.1    Barrington, S.F.2
  • 46
    • 77955466323 scopus 로고    scopus 로고
    • Initial experience with 18F-fluoroethylcholine PET/CT in staging and monitoring therapy response of advanced renal cell carcinoma
    • Middendorp M, Maute L, Sauter B, Vogl T, Grünwald F. Initial experience with 18F-fluoroethylcholine PET/CT in staging and monitoring therapy response of advanced renal cell carcinoma. Ann Nucl Med 2010;24:441-6.
    • (2010) Ann Nucl Med , vol.24 , pp. 441-446
    • Middendorp, M.1    Maute, L.2    Sauter, B.3    Vogl, T.4    Grünwald, F.5
  • 48
    • 33747893488 scopus 로고    scopus 로고
    • In vivo biological activity of the histone deacetylase inhibitor LAQ824 is detectable with 3'-deoxy-3'-[18F]fluorothymidine positron emission tomography
    • Leyton J, Alao JP, Da Costa M, Stavropoulou AV, Latigo JR, Perumal M, et al. In vivo biological activity of the histone deacetylase inhibitor LAQ824 is detectable with 3'-deoxy-3'-[18F]fluorothymidine positron emission tomography. Cancer Res 2006;66:7621-9.
    • (2006) Cancer Res , vol.66 , pp. 7621-7629
    • Leyton, J.1    Alao, J.P.2    Da Costa, M.3    Stavropoulou, A.V.4    Latigo, J.R.5    Perumal, M.6
  • 49
    • 79960912286 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor PXD101 increases the efficacy of irinotecan in in vitro and in vivo colon cancer models
    • Na YS, Jung KA, Kim SM, Hong YS, Ryu MH, Jang SJ, et al. The histone deacetylase inhibitor PXD101 increases the efficacy of irinotecan in in vitro and in vivo colon cancer models. Cancer Chemother Pharmacol 2011;68:389-98.
    • (2011) Cancer Chemother Pharmacol , vol.68 , pp. 389-398
    • Na, Y.S.1    Jung, K.A.2    Kim, S.M.3    Hong, Y.S.4    Ryu, M.H.5    Jang, S.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.